FDA applicant
Siemens Life Support Systems
FDA records 6 decisions for Siemens Life Support Systems (Schaumburg, IL) from 1989 to 1991: 6 510(k) clearances. Most are in product codes CBK (Ventilator, Continuous, Facility Use) and BRY (Cabinet, Table And Tray, Anesthesia). 3 recalls are linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Siemens Life Support Systems’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Siemens Life Support Systems since 2007.
Recalls per year
2in 2009
Class I Class II/III not classified
Planning a device like Siemens Life Support Systems’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
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